Trifluoroacetic acid → Methyl 5-amino-6-(1H-imidazol-1-yl)nicotinate

Compounds 64C1 and 64C2: 3-(Hydroxymethyl)imidazo[1,2-a]pyrido[3,2-e]pyrazin-6(5H)-one and 3-(Hydroxymethyl)imidazo[1,5-a]pyrido[3,2-e]pyrazin-6(5H)-one: Methyl 6-oxo-5,6-dihydroimidazo[1,2-a]pyrido[3,2-e]pyrazine-3-carboxylate (0.410 g, 1.68 mmol) was suspended in THF (20 mL) and sodium hydride (60% susp. in mineral oil, 0.112 g, 2.80 mmol) was added in one portion. The reaction mixture was stirred at room temperature for 1 h, cooled to −50° C. and LiAlH4 (2M in THF, 1.7 mL, 3.4 mmol) was added dropwise over 2 min. The reaction mixture was kept at −30-(−10)° C. for 3 h and more LiAlH4 (2M in THF, 0.7 mL and 1.0 mL, 3.4 mmol combined) was added. The reaction mixture was cooled to −60° C. and slowly quenched with MeOH, warmed to room temperature and TFA and water were added until a clear solution resulted. The solution was subjected to preparative HPLC (1-30% acetonitrile in water, TFA buffered) to afford the title compound as a grey solid (147 mg, 40%; ˜2:1 mixture of imidazole regioisomers). [M+H] calc'd for C10H8N4O2, 217; found, 217.

1. temperaturecooled to −50° C.
2. waitfor 3 h
3. temperatureThe reaction mixture was cooled to −60° C.
4. customslowly quenched with MeOH
5. temperaturewarmed to room temperature
6. additionTFA and water were added until a clear solution
7. customresulted

ORD record

ord-4ed2ba6dc88e4c6f8f9d4e5bf8d1112c

Source dataset

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08822470B2